Evidence map›Paper›PMID 31026677›Full record

ArticleMolecular therapy. Nucleic acids2019

Modulation of the IL-6-Signaling Pathway in Liver Cells by miRNAs Targeting gp130, JAK1, and/or STAT3.

Florence A Servais, Mélanie Kirchmeyer, Matthias Hamdorf, Nadège W E Minoungou, Stefan Rose-John, Stephanie Kreis, Claude Haan, Iris Behrmann

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.3field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. F1000Research · 2022
    Article
  11. Review
  12. Cholangiocarcinoma.Nature reviews. Disease primers · 2021
    Review
  13. The miRNA: a small but powerful RNA for COVID-19.Briefings in bioinformatics · 2021
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 2 countries.

Florence A ServaisSignal Transduction Laboratory, Life Sciences Research Unit, University of Luxembourg, 6, Avenue du Swing, 4367 Belvaux, Luxembourg.
Mélanie KirchmeyerSignal Transduction Laboratory, Life Sciences Research Unit, University of Luxembourg, 6, Avenue du Swing, 4367 Belvaux, Luxembourg.
Matthias HamdorfSignal Transduction Laboratory, Life Sciences Research Unit, University of Luxembourg, 6, Avenue du Swing, 4367 Belvaux, Luxembourg.
Nadège W E MinoungouSignal Transduction Laboratory, Life Sciences Research Unit, University of Luxembourg, 6, Avenue du Swing, 4367 Belvaux, Luxembourg.
Stefan Rose-JohnInstitute of Biochemistry, Christian-Albrechts-Universität zu Kiel, Medical Faculty, Olshausenstraße 40, 24098 Kiel, Germany.
Stephanie KreisSignal Transduction Laboratory, Life Sciences Research Unit, University of Luxembourg, 6, Avenue du Swing, 4367 Belvaux, Luxembourg.
Claude HaanSignal Transduction Laboratory, Life Sciences Research Unit, University of Luxembourg, 6, Avenue du Swing, 4367 Belvaux, Luxembourg.
Iris BehrmannSignal Transduction Laboratory, Life Sciences Research Unit, University of Luxembourg, 6, Avenue du Swing, 4367 Belvaux, Luxembourg. Electronic address: iris.behrmann@uni.lu.
University of Luxembourg · LUKiel University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukin-6 (IL-6)-type cytokines share the common receptor glycoprotein 130 (gp130), which activates a signaling cascade involving Janus kinases (JAKs) and signal transducer and activator of transcription (STAT) transcription factors. IL-6 and/or its signaling pathway is often deregulated in diseases, such as chronic liver diseases and cancer. Thus, the identification of compounds inhibiting this pathway is of interest for future targeted therapies. We established novel cellular screening systems based on a STAT-responsive reporter gene (Cypridina luciferase). Of a library containing 538 microRNA (miRNA) mimics, several miRNAs affected hyper-IL-6-induced luciferase activities. When focusing on candidate miRNAs specifically targeting 3' UTRs of signaling molecules of this pathway, we identified, e.g., miR-3677-5p as a novel miRNA affecting protein expression of both STAT3 and JAK1, whereas miR-16-1-3p, miR-4473, and miR-520f-3p reduced gp130 surface expression. Interestingly, combination treatment with 2 or 3 miRNAs targeting gp130 or different signaling molecules of the pathway did not increase the inhibitory effects on phospho-STAT3 levels and STAT3 target gene expression compared to treatment with single mimics. Taken together, we identified a set of miRNAs of potential therapeutic value for cancer and inflammatory diseases, which directly target the expression of molecules within the IL-6-signaling pathway and can dampen inflammatory signal transduction.

Indexed as

cancercytokinegp130inflammationinterleukin-6JAK1livermicroRNAssignal transductionSTAT3

Identifiers

PMID31026677
PMCPMC6479786
OpenAlexW2926364724

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.